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A One-pot process for the synthesis of Alkyne-3-tretrazolyl-tetrazolo [1,5-a] quinolines.
Published:
14 November 2018
by MDPI
in The 22nd International Electronic Conference on Synthetic Organic Chemistry
session General Organic Synthesis
Abstract:
An efficient synthesis of alkyne-3-tetrazolyl-Tetrazolo[1,5-a] quinolone via a one-pot process: I-MCR Ugi-azide /SNAr/ ring-chain azido tautomerization under ecofriendly conditions. We report the one-pot synthesis of tris-heterocycles containing the tetrazolo[1,5-a]quinoline bound with 1,5-disubstituted-tetrazole (1,5-DS-T). The synthesis of this compounds can be of high interest for synthetic and medicinal chemistry because all the heterocycles are considered privilegied scaffolds and could lead to the discovery of novel bioactive molecules.
Keywords: Isocyanide based multicomponent reactions; Ugi-azide; Tetrazolo [1,5-a] quinolines; ring-chain azido tautomerization; one-pot process.